Mutation of the Emx-1 homeobox gene disrupts the corpus callosum

被引:87
作者
Qiu, MS
Anderson, S
Chen, SD
Meneses, JJ
Hevner, R
Kuwana, E
Pedersen, RA
Rubenstein, JLR
机构
[1] UNIV CALIF SAN FRANCISCO,DEPT PSYCHIAT,CTR NEUROBIOL & PSYCHIAT,NINA IRELAND LAB DEV NEUROBIOL,SAN FRANCISCO,CA 94143
[2] UNIV CALIF SAN FRANCISCO,PROGRAM NEUROSCI,SAN FRANCISCO,CA 94143
[3] UNIV CALIF SAN FRANCISCO,PROGRAM DEV BIOL,SAN FRANCISCO,CA 94143
[4] UNIV CALIF SAN FRANCISCO,LAB RADIOBIOL & ENVIRONM HLTH,SAN FRANCISCO,CA 94143
[5] UNIV CALIF SAN FRANCISCO,DEPT OBSTET GYNECOL & REPROD SCI,SAN FRANCISCO,CA 94143
关键词
D O I
10.1006/dbio.1996.0207
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Expression of the Emx-1 homeobox gene is largely restricted to the developing and mature cerebral cortex. To study its function, two lines of mice were generated using gene targeting methods that have a deletion that includes the N-terminal coding region of Emx-1. Mice homozygous for the deletion were viable and fertile and exhibited no obvious behavioral defects, However, 100% of homozygous mice lack most or all of their corpus callosum, the principle fiber tract that connects the left and right cerebral hemispheres. Heterozygotes show partial penetrance for the corpus callosum abnormality, The histology and various molecular properties of the cerebral cortex appear normal in the mutant mice. (C) 1996 Academic Press, Inc.
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收藏
页码:174 / 178
页数:5
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